| Tag | Content |
|---|
EnhancerAtlas ID | HS091-22964 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:4850700-4852020 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr19:4851800-4851819 | AGGCGCCCTCTGGTGGCTG | - | 7.12 | | Hnf4a | MA0114.3 | chr19:4851722-4851738 | CTTGGGCTTTGACCCC | - | 6.3 | | ZNF263 | MA0528.1 | chr19:4851653-4851674 | GGGGGAAGAGGAGGAGGGCGG | + | 6.25 | | ZNF263 | MA0528.1 | chr19:4851650-4851671 | GAAGGGGGAAGAGGAGGAGGG | + | 6.67 | | ZNF263 | MA0528.1 | chr19:4851662-4851683 | GGAGGAGGGCGGGGAGAGGAC | + | 6.76 | | ZNF263 | MA0528.1 | chr19:4851659-4851680 | AGAGGAGGAGGGCGGGGAGAG | + | 7.17 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_06599 | chr19:4851186-4852834 | Brain_Hippocampus_Middle | | SE_27604 | chr19:4851512-4852052 | Esophagus |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I004851 | chr19 | 4851681 | 4851890 |
|
Enhancer Sequence | CCTCCCAAAG TGCTGGGATT ACAGGCGTGA CCCACCGTGC CCGGCCTAAT TTTTGTATTT 60
TTAGTAGAGA CCGGGTTTCA CCATGTTGGC CAGGCTTGTC TCAAACTCTT GACTTCAGGT 120
GATCTGCCCA CCTCGGCCCA CCAAAGTGCT GGGATTACAG GCTGAGCCAC CGCGCCCTGC 180
CTATATCCTA AGCTACTTAT TTGCAAAAAT CCCAATCCCC GCACTTTGGG GGGCTAAAGC 240
AGTAGGATCA CTCCAGCCAA GGAGTTCTGG ATCAGCTGGG ATGACAGAGG GAGACCCCGT 300
CTTTACCAAA AATTAAATAA AGAAAAATTA GTTGGGCGTG ATGGTGTGTG CTTGTAGTCC 360
CAGCTACTCG GAGGCTGAGA TGGGAGGCTC GCCTCAACCC AGGAGTTGGA GGCTGCATTG 420
AGCTATGATC GCACCACTGC ACTTCAGCCT GGGCAAGAGA GTGAGACTCT ATCTCTAAAA 480
CAAATAAATA AAAAAGGGCC GGGCATGGTG GCTCACACCT GTAATCCCAG TACTTGGGGA 540
GGCCGAGGTG GGCAGATCAC AAGGTCAGGA GTTCGAGACC AGCCTGGCCA ACATAGTGAA 600
ACCCCGTTTC TACTAAAAAT ACAAAAAATT AGCTGTGTGG TGGCAGGTGC CTGTAATCCC 660
AGCTACTCAG GAGGATGAGG CAGGAGACTC GCTTGAACCC AGGAGGCAGA GGTTGCAGTG 720
AGCTGAGATC ACGCCATTGC ACTCCAGCCT AGGTGACAGG GCGAGACTCT GTCTCTAAAT 780
AAATAAATAA ATTAATTAAA GAAGAATATC AAATAAACAG TGCAGGGAGT GCGAATATGT 840
GACCGAGATG ACTGGAGTGG GATGTCTGGC CTGGCGGGAA CACCAGCATT GTTGTCACAG 900
TTCAGTGAGA TCTCAAGTTT AGTCACGTAT TTATGCAGGA GCGGAGTGGC GAAGGGGGAA 960
GAGGAGGAGG GCGGGGAGAG GACAGGGGAG GTTGTGCAGG ACCTTGTGGG CTGTGACGAG 1020
GACTTGGGCT TTGACCCCAG GGGAGGTGGG GTCCATGGAG GGCTGTGGGC AGAGGGACGG 1080
GTTCTGACTC AGGTGGTCAC AGGCGCCCTC TGGTGGCTGC TGTGGGGAGG AGACTGTGGT 1140
GGATGAGGGC GGGAGCTGGT GAGCAGGACA GAGGGGACTG CGTTAGTGAT GAGATTCCAA 1200
GATGCCCGGG AGAAGTGGCA GGGACGAGGC GGCAGTGAGT GTCGGCACAG ACCCCAGGAG 1260
GCCGACAGCG GCTTCCGGTC AGGGGGCCTG GGGAGGGGTC CCAGAGCAGC CCGCTGGCCA 1320
|
